Evidence map›Paper›PMID 28829742›Full record

ArticleeLife2017

Inhibition of Transient Receptor Potential Melastatin 3 ion channels by G-protein βγ subunits.

Doreen Badheka, Yevgen Yudin, Istvan Borbiro, Cassandra M Hartle, Aysenur Yazici, Tooraj Mirshahi, Tibor Rohacs

Open access · goldAbstract read
In one paragraph

Article in eLife, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
6.1field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

58 citing papers in PubMed, 85 citations in OpenAlex.

  1. Trial
  2. GluDs are ionotropic dopamine receptors tuned by G-proteins.bioRxiv : the preprint server for biology · 2026
    Article
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  6. Review
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  11. Article
  12. Navigating the Controversies: Role of TRPM Channels in Pain States.International journal of molecular sciences · 2024
    Review
  13. TRPM3, TRPM4, and TRPM5 as thermo-sensitive channels.The journal of physiological sciences : JPS · 2024
    Review
  14. Article
  15. Article
  16. Article
  17. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Doreen BadhekaNew Jersey Medical School, Rutgers, the State University of New Jersey, Newark, United States.
Yevgen YudinNew Jersey Medical School, Rutgers, the State University of New Jersey, Newark, United States.
Istvan BorbiroNew Jersey Medical School, Rutgers, the State University of New Jersey, Newark, United States.ORCID 0000-0002-8366-6881
Cassandra M HartleDepartment of Molecular and Functional Genomics, Weis Center for Research, Geisinger Clinic, Danville, United States.
Aysenur YaziciNew Jersey Medical School, Rutgers, the State University of New Jersey, Newark, United States.
Tooraj MirshahiDepartment of Molecular and Functional Genomics, Weis Center for Research, Geisinger Clinic, Danville, United States.
Tibor RohacsNew Jersey Medical School, Rutgers, the State University of New Jersey, Newark, United States.ORCID 0000-0003-3580-2575
Rutgers, The State University of New Jersey · USGeisinger Medical Center · US

Funding

Regulation of sensory TRP channels by phospholipids and G-proteinsR01NS055159 · NINDS · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI ROHACS, TIBOR · 2007 to 2022
$5.9M
Regulation of the Intestinal Ca2+ Channels TRPV6R01GM093290 · NIGMS · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI CARNEVALE, VINCENZO, ROHACS, TIBOR · 2011 to 2025
$4.9M
An integrated approach to study GPCR variants associated with complex diseasesR01GM111913 · NIGMS · GEISINGER CLINIC · PI MIRSHAHI, TOORAJ, ROBISHAW, JANET D · 2015 to 2018
$2.1M
Molecular mechanism of TRPV1 activationR01GM131048 · NIGMS · TEMPLE UNIV OF THE COMMONWEALTH · PI CARNEVALE, VINCENZO, ROHACS, TIBOR · 2019 to 2022
$1.4M
NIGMS NIH HHS R01 GM093290NIGMS NIH HHS R01 GM111913NIGMS NIH HHS R01 GM131048NINDS NIH HHS R01 NS055159
6 · The paper itself

Abstract

Transient receptor potential melastatin 3 (TRPM3) channels are activated by heat, and chemical ligands such as pregnenolone sulphate (PregS) and CIM0216. Here, we show that activation of receptors coupled to heterotrimeric Gi/o proteins inhibits TRPM3 channels. This inhibition was alleviated by co-expression of proteins that bind the βγ subunits of heterotrimeric G-proteins (Gβγ). Co-expression of Gβγ, but not constitutively active Gαi or Gαo, inhibited TRPM3 currents. TRPM3 co-immunoprecipitated with Gβ, and purified Gβγ proteins applied to excised inside-out patches inhibited TRPM3 currents, indicating a direct effect. Baclofen and somatostatin, agonists of Gi-coupled receptors, inhibited Ca

Indexed as

AnimalsBaclofenBehavior Rating ScaleCalciumGanglia, SpinalGTP-Binding Protein alpha Subunits, Gi-GoGTP-Binding Protein beta SubunitsGTP-Binding Protein gamma SubunitsHEK293 CellsHeterocyclic Compounds, 4 or More RingsHumansIntracellular Signaling Peptides and ProteinsMiceNeuronsPregnenoloneSomatostatinBaclofenCalciumCIM0216GINIP protein, ratGNAO1 protein, mouseG-protein Beta gammaGTP-Binding Protein alpha Subunits, Gi-GoGTP-Binding Protein beta SubunitsGTP-Binding Protein gamma SubunitsHeterocyclic Compounds, 4 or More RingsIntracellular Signaling Peptides and ProteinsPregnenolonepregnenolone sulfateSomatostatinTRPM3 protein, mouseTRPM Cation ChannelsDRG neuronG-proteinmouseneurosciencesensory ion channelTRPA1TRPM3TRPM8

Identifiers

PMID28829742
PMCPMC5593506
OpenAlexW2747808331

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.